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Results 1 - 9 of 9 for Hereditary spastic paraplegia 28
  1. Spastic paraplegia type 4 
    ... UK and Irish HSP Consortium. Clinical features of hereditary spastic paraplegia due to spastin mutation. Neurology. 2006 Jul 11;67(1):45-51. doi: 10.1212/01.wnl.0000223315.62404.00. Erratum In: Neurology. 2009 Apr 28;72(17):1534. Citation on PubMed Rattay TW, ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-4 - Genetics
  2. Spastic paraplegia type 7 
    ... each cell is sufficient to cause the disorder. Hereditary spastic paraplegia, paraplegin type Spastic paraplegia 7 Genetic Testing Registry: Hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia 7 Hereditary ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  3. Spastic paraplegia type 5A 
    ... Spastic paraplegia type 5A is usually a pure hereditary spastic paraplegia, although complex type features have been reported in ... 5A Spastic paraplegia 5A SPG5A Genetic Testing Registry: Hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia 5A Autosomal ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-5a - Genetics
  4. Fatty acid hydroxylase-associated neurodegeneration 
    ... paraparesis FAHN Spastic paraplegia 35 Genetic Testing Registry: Hereditary spastic paraplegia 35 Fatty acid hydroxylase-associated neurodegeneration National Organization ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  5. SPG7 gene 
    ... deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J Cell Biol. 2003 Nov 24;163(4): ... genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia. Brain. 2004 May;127(Pt 5):973-80. ...
    https://medlineplus.gov/genetics/gene/spg7 - Genetics
  6. C19orf12 gene 
    ... individuals are considered to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition NBIA3 ... Zuchner S, Blackstone C, Fischbeck KH, Burnett BG. Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  7. Troyer Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Troyer syndrome (also known as spastic paraplegia gene, SPG20) belongs to a group of nervous system disorders called hereditary spastic paraplegias. The main feature of these disorders are muscle weakness and spasms in the legs that tend to get worse over ...
    https://www.ninds.nih.gov/.../disorders/troyer-syndrome - External Health Links
  8. TUBB4A-related leukodystrophy 
    ... TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  9. FA2H gene 
    ... Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35). Hum Mutat. 2010 Apr;31(4):E1251- ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics